Thrombocytopenia

Ci fai o ci SEU?

Benigni G, Verticelli T, Pugliese F

2026/3 — pag. 72-73 — DOI

Haemolytic Uremic Syndrome (HUS) is a thrombotic microangiopathy frequently triggered by Shiga toxin-producing E. coli (STEC). This report compares two paediatric cases caused by the same pathogen (E. coli O157:H7) with divergent clinical outcomes. I...

Piastrinopenia nel contesto di una intercorrenza infettiva

Zago A

2025/10 — pag. 275-276 — DOI

The paper reports the case of a 10-year-old girl with acute post-infectious thrombocytopenia, presenting with widespread petechiae, ecchymoses and epistaxis, with otherwise normal blood counts. Initial platelet count was 0/mm³. Intravenous immunoglob...

Occhio all'emocromo... prima che sia tardi

Di Noto F, Lo Meo F, Marra G, Dimartino G, Gilotta C, Genduso M, Ferraro T, Allegra M, Guarina A, Cardella F, Corsello G

2025/7 — pag. 190-191 — DOI

A 5-year-old boy, presented with hematemesis, diffuse petechiae, epistaxis, respiratory distress and severe pancytopenia. After poor response to immunoglobulin and steroid therapy, bone marrow evaluation revealed trilineage cytopenia. The combination...

Un neonato con piastrinopenia

Starita A

2025/7 — pag. 179-181 — DOI

The paper describes the case of newborn with thrombocytopenia. The final diagnosis is a rare, potentially severe disease that, therefore, should be promptly recognised....

Rivista sfogliabile on line

2024/10

Una trombocitopenia associata alla scabbia in un neonato: caso clinico e revisione della letteratura

Giulia La Malfa

2024/10 — pag. 220-222 — DOI

The paper presents the case of a 1-month-old infant with persistent skin lesions who was diagnosed with scabies after initial ineffective treatments. The condition was linked to thrombocytopenia and anaemia, which resolved following dermatologic ther...

Una strana pancitopenia: dalla gestione in urgenza alla diagnosi genetica

Di Filippo M, Rossoni L, Nebiolo M, Fioredda F, Carrato V, Pirlo D

2024/10 — pag. 201-206 — DOI

Wiskott-Aldrich syndrome (WAS) is a rare X-linked genetic disorder caused by a mutation in the WAS gene that codes for the WASp protein, which is involved in the functioning of the cytoskeleton of non-erythroid haematopoietic cells. This mutation lea...

Infezione da virus di Epstein-Barr: citopenia e colecisti ispessita

Benvenuto S.

2023/4 — pag. 260 — DOI

The author describes the case of a 13-year-old girl presenting with abdominal pain, thrombocytopoenia and neutropoenia. A thickened gallbladder was evident at abdominal sonography. The diagnosis of EBV infection, based on serological investigation, w...

Un caso insolito di trombocitopenia

Barachino A

2023/1 — pag. 4-5 — DOI

A two-and-a-half-year-old child presents with spontaneous ecchymosis. In addition to severe thrombocytopoenia, initial investigations show the presence of neutropoenia and signs of immune-mediated haemolysis (positivity of the direct antiglobulin tes...

Quando la malaria tarda a farsi riconoscere: un’infezione da Plasmodium ovale

Polenzani I, Lisco L, Cozzolino M, Casolari S, Valenti S, Fontijn S, Uva A, Marchetti F.

2022/6 — pag. 381-385 — DOI

Plasmodium ovale is a cause of non-falciparum malaria infection that is endemic in tropical Western Africa. The life cycle of Plasmodium ovale includes hypnozoites, which are dormant stages in the liver. These stages can be reactivated after weeks, m...

CAMT: trombocitopenia amegacariocitica congenita

V. Carrato

2020/9 — pag. 239-239 — DOI

Diarrea ematica nel bambino… pensa alla sindrome emolitico-uremica!

R. Letizia, G. Maiorino, M.E. Di Cicco, G.I. Baroncelli, E. De Marco, D. Peroni

2020/7 — pag. 180-185 — DOI

A healthy 5-year-old boy was brought to the Emergency Department with a 24-hour-history of fever, abdominal pain, bloody diarrhoea and vomiting. Blood tests and ultrasound of the abdomen suggested an acute gastroenteritis. The boy was admitted and in...

Prima la piastrinopenia poi l’embolia polmonare

F. Marchetti, C. Radice, L. Biserna, A.C. Nuzzo, L. Mambelli

2019/10 — pag. 631-633

The paper describes the case of a 17-year-old girl presenting with an initial diagnosis of severe idiopathic thrombocytopoenic purpura with negative ANA and positive Coombs test. After a first phase characterised by thrombocytopeonia with haemorrha...

LA COMPLESSITÀ DEL LUPUS ERITEMATOSO SISTEMICO

A. Taddio

2019/10 — pag. 627

Cerchi una celiachia, trovi... una leucemia

S. Molinari

2018/6

Piastrinopenia immunomediata in età adolescenziale ed evoluzione in lupus eritematoso sistemico

G. Costagliola, R. Consolini

2018/2 — pag. 97-100

Thrombocytopenia, defined by a platelet count lower than 100,000 mm3, in children and adolescents is more frequently ascribable to an immune pathogenesis (Immune Thrombocytopenia, or ITP). ITP is defined “persistent” if it is still present after th...

Una ragazza con ascite e diarrea con sangue: quale diagnosi?

F. Marchetti, M. Mainetti, M. Giovannini, C. Morelli

2017/8 — pag. 519-522

Due storie di malaria: c’è sempre da imparare

M.T. Bartolini, C. Ghizzi

2017/8

Due zoppie per due diagnosi

F. Corrias

2017/7 — pag. 465-466

MAS in WAS? (una Wiskott-Aldrich non convenzionale)

S. Amoroso

2016/10

Quando le piastrine basse possono... attendere

E. Mazzoni, F. Lombardi, C. Fochi, A. Lambertini

2016/5 — pag. 316-318

La sindrome di Evans: chi è costei?

F. Pugliese, A. Zucchini, R. Burnelli, F. Marchetti

2015/7

Il sale della vita: esami di laboratorio nelle IVU?

G. Bassanese, S. Norbedo, M. Pennesi

2014/5

Severe hyponatremia has been reported as a possible complication in children with renal dysplasia and urinary tract infection (UTI). The pathogenesis of this conditions is probably due to concomitant events such as renal parenchima flogosis and the i...

Al di là dell’occhio!

G. Ferrara, E. Zanelli

2014/3

Piastrine che scendono, piastrine che salgono: quando preoccuparsi?

E. Parodi, G. Ansaldi, C. Botto, M. Davitto, A. Mondino, C. Olivieri, U. Ramenghi

2013/10 — pag. 629-634

Thrombocytopenia and thrombocytosis are defined by a decreased or an elevated platelet count, respectively. Changes in the platelet number are frequently observed during childhood. This article aims at quickly examining the main causes of thrombocy...

Non sempre epistassi ed ecchimosi indicano una porpora

G. Sanna, D. Ticca, V. Manca, L. Buono

2012/7

Trombocitopenia da acido valproico o da infezione virale?

E. Gnoato, S. Masiero, C. Moretti

2012/6

Un male dell'altro mondo

S. Lasagni, G. Boschi, I. Dodi, M.A. Bandello, A. Defanti, S. Amarri

2012/5

Caverne

E. Ugolini, P. Fioretti

2012/4 — pag. 259-260

Una banale gastroenterite?

A. Paladini, S. Ciccone, C. Farneti

2010/10

Addome acuto a sorpresa

I. Giuseppin, M. Ranieri, P. Flora

2010/3

Quando le vitamine servono davvero

F. Lombardi, A.L. Quitadamo, A. Pelizzoni, P. Accorsi, F. Olivetti

2010/2

Un caso di zoppia

C. Galletto, N. Bertorello, E. Barisone, R. Mazzone, A. Andreacchio

2007/1

Un caso di polmonite con piastrinosi

F. De Maddi, C. Santoro, R. Crusco, P. Siani

2006/10

Una bambina con artrite reumatoide sistemica e febbre: è una ricaduta?

C. Oretti, M. Maschio, M. Lazzerini

2004/9

PIastrinopenia isolata x-linked da mutazione missense del gene Wasp: descrizione di un caso

C Locatelli, C Malaventura, R Ciambra, M Pocecco, L. D Notarangelo, L. D Notarangelo

2004/7

Piastrinopenia isolata X-linked da mutazione del gene WASP

2004/7 — pag. 450-450

Wiskott-Aldrich (WAS) and X-linked thrombocytopenia (XLT) are two disorders caused by different mutations of the gene WASP. WAS is characterized by recurrent infections, eczema, thrombocytopenia with low mean platet volume (MPV) and increased sus...

Desametazone ad alte dosi nella porpora trombocitopenica immune

G. Bartolozzi

2003/8

Piastrinopenia cronica multiresistente in bambina con sindrome linfoproliferativa autoimmune (ALPS). Efficacia della ciclofosfamide

E. Barth, M. Rabusin G.A. Zanazzo, P. Tamaro

2001/8

Un caso clinico dalla letteratura internazionale, con integrazioni patogenetico-cliniche

G. Bartolozzi

2001/8

Piastrinopenia cronica multiresistente in bambina con sindrome linfoproliferativa autoimmune (ALPS): efficacia della ciclofosfamide

E. Barth, M. Rabusin, GA. Zanazzo, P. Tamaro

2001/8 — pag. 548-548

Report of a very severe case of thrombocytopenia with lymphoproliferative autoimmune syndrome (hereditary ALPS) resistant to classical treatments, both in high doses or bolus, with prompt and durable response to cyclophosfamide....

Un caso di polmonite “tipica” da mycoplasma

L. Gnemmi, M. Pocecco

1999/4

Un caso di polmonite tipica da mycoplasma

L. Gnemmi, M. Pocecco

1999/4 — pag. 217-218

La sindrome CFC (Cardio-facio-cutaneous syndrome): un caso con piastrinopenia

A. Borrelli, G. Pinto

1999/3

L'eczema di Piero

F. Fusco

1999/3 — pag. 191-192

La sindrome cfc: un caso con piastrinopenia

A. Borrelli, G. Pinto

1999/3 — pag. 149

La trombopoietinaFibrosi cistica e iperossaluriaQuale cura per la fimosi ?

G. Bartolozzi

1998/9